1. Academic Validation
  2. Diallyl trisulfide inhibits naphthalene-induced oxidative injury and the production of inflammatory responses in A549 cells and mice

Diallyl trisulfide inhibits naphthalene-induced oxidative injury and the production of inflammatory responses in A549 cells and mice

  • Int Immunopharmacol. 2015 Dec;29(2):326-333. doi: 10.1016/j.intimp.2015.10.033.
Fang Zhang 1 Yongchun Zhang 2 Kaiming Wang 1 Xiaosong Zhu 1 Guimei Lin 1 Zhongxi Zhao 3 Shanzhong Li 4 Jianhua Cai 4 Jimin Cao 4
Affiliations

Affiliations

  • 1 School of Pharmaceutical Sciences, Shandong University, 44 West Wenhua Road, Jinan 250012, PR China.
  • 2 School of Pharmaceutical Sciences, Shandong University, 44 West Wenhua Road, Jinan 250012, PR China; School of Chemistry and Pharmaceutical Engineering, Qilu University of Technology, Daxue Road, Western University Science Park, Jinan, Shandong 250353, PR China.
  • 3 School of Pharmaceutical Sciences, Shandong University, 44 West Wenhua Road, Jinan 250012, PR China; Jiangsu Shengshi Kangde Biotech Corporation, Lianyungang, Jiangsu 222006, PR China. Electronic address: [email protected].
  • 4 Jiangsu Shengshi Kangde Biotech Corporation, Lianyungang, Jiangsu 222006, PR China.
Abstract

Diallyl trisulfide (DATS) is a garlic organosulfide that may have a therapeutic potential in the treatment of some diseases. We sought to determine whether DATS could inhibit naphthalene-induced oxidative injury and the production of inflammatory responses in vitro and in vivo. A549 cells were either pre-treated (PreTx, prevention) or concurrently treated (CoTx, treatment) with 20μM naphthalene and either 5 or 10μM DATS. PreTx and CoTx showed the prevention and the treatment potential of DATS to inhibit the generation of naphthalene-induced Reactive Oxygen Species (ROS) in the A549 cells. DATS showed antioxidative activity by elevating the SOD activities in the low dose groups. The mechanistic study showed that the DATS-mediated inhibition of naphthalene-induced oxidative injury and the production of inflammatory responses (i.e., TNF-α, IL-6, and IL-8) were attributed to inhibiting the activity of nuclear factor-kappa B (NF-κB). In addition, DATS inhibited the production of serum nitric oxide NO and myeloperoxidase (MPO) in the lungs of Kunming mice. The histological analysis results indicate that DATS inhibited the naphthalene-induced lung damage, which is consistent with the in vitro study results. The in vivo and in vitro results suggest that DATS may be an effective attenuator of naphthalene-induced lung damage.

Keywords

Diallyl trisulfide; Inflammatory responses; Naphthalene; Nuclear factor-kappa B (NF-κB); Oxidative injury.

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